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FDA Inspection 1013345 — Biolife Plasma Services

Biolife Plasma Services — FEI 1876554

The FDA completed an inspection of Biolife Plasma Services on April 27, 2017 in Grand Rapids, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 27, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

  • 1142760 (NAI Thu May 20 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 868868 (NAI Fri Mar 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 770123 (NAI Tue Feb 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 653623 (NAI Tue Mar 23 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources